Disior, Ltd.
FDA Regulatory Profile
Disior, Ltd. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Feb 26, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K253764 | ENOS Software Guided External Fixation System | Feb 26, 2026 |
| K250023 | SMART PCFD | Sep 29, 2025 |
| K240736 | SMART Bun-Yo-Matic X-Ray | Jul 2, 2024 |
| K240642 | SMART Bun-Yo-Matic CT | Jun 20, 2024 |
| K223757 | Bonelogic | Dec 8, 2023 |
| K203290 | Bonelogic | Feb 5, 2021 |